Variant report

Variant	nsv1014376
Chromosome Location	chr1:62976472-63181359
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1664)
CpG islands
(count:1039)
Chromatin interactive
region (count:70)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1664 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:62989615-62989964	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:63153014-63153399	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:63087554-63088043	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:63151020-63151226	K562	blood:	n/a	n/a
5	ARID3A	chr1:62982221-62982850	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:63155138-63157154	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:63089241-63089296	HepG2	liver:	n/a	n/a
8	ARID3A	chr1:63079529-63079891	HepG2	liver:	n/a	n/a
9	ARID3A	chr1:63153903-63154123	HepG2	liver:	n/a	n/a
10	ARID3A	chr1:62980657-62981059	HepG2	liver:	n/a	n/a
11	ARID3A	chr1:63155854-63156261	K562	blood:	n/a	n/a
12	ARID3A	chr1:63004676-63005485	K562	blood:	n/a	n/a
13	ARID3A	chr1:63074554-63075140	HepG2	liver:	n/a	n/a
14	ARID3A	chr1:63059494-63060018	HepG2	liver:	n/a	chr1:63059505-63059521
15	ATF1	chr1:63155923-63156556	K562	blood:	n/a	n/a
16	ATF1	chr1:63087652-63087993	K562	blood:	n/a	n/a
17	ATF1	chr1:63148145-63148210	K562	blood:	n/a	n/a
18	ATF1	chr1:63004842-63005160	K562	blood:	n/a	n/a
19	ATF2	chr1:63087593-63087996	GM12878	blood:	n/a	n/a
20	ATF2	chr1:63078872-63079532	GM12878	blood:	n/a	n/a
21	ATF2	chr1:63087614-63088085	GM12878	blood:	n/a	n/a
22	ATF2	chr1:63153966-63154538	H1-hESC	embryonic stem cell:	n/a	n/a
23	ATF3	chr1:63087530-63087957	A549	lung:	n/a	n/a
24	ATF3	chr1:63087496-63087981	A549	lung:	n/a	n/a
25	ATF3	chr1:63087594-63087996	K562	blood:	n/a	n/a
26	ATF3	chr1:63155903-63156411	K562	blood:	n/a	n/a
27	BATF	chr1:63064713-63065027	GM12878	blood:	n/a	chr1:63064849-63064860
28	BATF	chr1:63087603-63088001	GM12878	blood:	n/a	n/a
29	BATF	chr1:63087655-63088035	GM12878	blood:	n/a	n/a
30	BATF	chr1:63091155-63091470	GM12878	blood:	n/a	n/a
31	BATF	chr1:63064757-63064998	GM12878	blood:	n/a	chr1:63064849-63064860
32	BCL11A	chr1:63087711-63088043	GM12878	blood:	n/a	n/a
33	BCL11A	chr1:63091142-63091436	GM12878	blood:	n/a	n/a
34	BCL3	chr1:63087446-63088045	A549	lung:	n/a	n/a
35	BCLAF1	chr1:63153878-63154436	GM12878	blood:	n/a	chr1:63154385-63154394
36	BCLAF1	chr1:63153932-63154386	GM12878	blood:	n/a	n/a
37	BCLAF1	chr1:63078822-63079525	GM12878	blood:	n/a	chr1:63079303-63079312
38	BCLAF1	chr1:63155871-63156403	K562	blood:	n/a	n/a
39	BHLHE40	chr1:63087617-63088019	K562	blood:	n/a	n/a
40	BHLHE40	chr1:63156016-63157064	HepG2	liver:	n/a	n/a
41	BHLHE40	chr1:63078977-63079505	GM12878	blood:	n/a	n/a
42	BHLHE40	chr1:63097743-63097749	GM12878	blood:	n/a	n/a
43	BHLHE40	chr1:63153099-63153368	K562	blood:	n/a	n/a
44	BHLHE40	chr1:63087611-63088010	GM12878	blood:	n/a	n/a
45	BHLHE40	chr1:63087555-63087977	HepG2	liver:	n/a	n/a
46	BHLHE40	chr1:63153877-63154737	K562	blood:	n/a	chr1:63154459-63154475
47	BHLHE40	chr1:63151475-63151537	K562	blood:	n/a	n/a
48	BHLHE40	chr1:63155883-63156310	K562	blood:	n/a	n/a
49	BHLHE40	chr1:63140350-63140418	GM12878	blood:	n/a	n/a
50	BHLHE40	chr1:63153813-63154292	GM12878	blood:	n/a	n/a

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:63043009-63043059	GM12892	blood:	n/a
2	chr1:63156450-63156500	BJ	skin:	n/a
3	chr1:63043009-63043059	GM12892	blood:	n/a
4	chr1:63156450-63156500	BJ	skin:	n/a
5	chr1:63062489-63062539	GM19239	blood:	n/a
6	chr1:63154320-63154370	HRE	kidney:	n/a
7	chr1:63154584-63154634	HepG2	liver:	n/a
8	chr1:63142359-63142409	HepG2	liver:	n/a
9	chr1:63062724-63062774	AG09309	skin:	n/a
10	chr1:63154465-63154515	AG10803	skin:	n/a
11	chr1:63154320-63154370	AG09309	skin:	n/a
12	chr1:63153194-63153244	HL-60	blood:	n/a
13	chr1:63004738-63004788	BJ	skin:	n/a
14	chr1:63154668-63154718	GM12892	blood:	n/a
15	chr1:63150905-63150955	AG09319	gingival:	n/a
16	chr1:63154465-63154515	Jurkat	blood:	n/a
17	chr1:63156450-63156500	MCF10A-Er-Src	breast:	n/a
18	chr1:63136405-63136455	HPAEpiC	pulmonary alveolar:	n/a
19	chr1:63154287-63154337	HEK293	kidney:	embryo
20	chr1:63151692-63151742	HEEpiC	esophagus:	n/a
21	chr1:63150905-63150955	K562	blood:	n/a
22	chr1:63142359-63142409	SK-N-MC	brain:	n/a
23	chr1:63062489-63062539	HIPEpiC	eye:	n/a
24	chr1:63043009-63043059	GM12878	blood:	n/a
25	chr1:63154668-63154718	HRE	kidney:	n/a
26	chr1:63151692-63151742	T-47D	breast:	n/a
27	chr1:63154320-63154370	HIPEpiC	eye:	n/a
28	chr1:63062724-63062774	MCF10A-Er-Src	breast:	n/a
29	chr1:63150905-63150955	IMR90	lung:	fetal
30	chr1:63062724-63062774	HNPCEpiC	eye:	n/a
31	chr1:63043009-63043059	GM19239	blood:	n/a
32	chr1:63136405-63136455	HCF	heart:	n/a
33	chr1:63151692-63151742	NHBE	bronchial:	n/a
34	chr1:63153804-63153854	NHDF-neo	bronchial:	n/a
35	chr1:63004738-63004788	HCM	heart:	n/a
36	chr1:63043009-63043059	HRCEpiC	kidney:	n/a
37	chr1:63154320-63154370	SAEC	small airway:	n/a
38	chr1:63154320-63154370	HCT-116	colon:	n/a
39	chr1:63142359-63142409	AG10803	skin:	n/a
40	chr1:63154668-63154718	HAEpiC	amniotic membrane:	n/a
41	chr1:63154287-63154337	T-47D	breast:	n/a
42	chr1:63043009-63043059	NT2-D1	testis:	n/a
43	chr1:63154320-63154370	HAEpiC	amniotic membrane:	n/a
44	chr1:63153804-63153854	GM06990	blood:	n/a
45	chr1:63153194-63153244	AG04450	lung:	fetal
46	chr1:63136405-63136455	RPTEC	kidney:	n/a
47	chr1:63062724-63062774	HCT-116	colon:	n/a
48	chr1:63062489-63062539	IMR90	lung:	fetal
49	chr1:63151692-63151742	MCF-7	breast:	n/a
50	chr1:63150905-63150955	PrEC	prostate:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:63119431..63121018-chr1:63143900..63145920,2	K562	blood:
2	chr1:63143255..63144801-chr1:63148236..63149930,2	K562	blood:
3	chr1:63146913..63149001-chr1:63152180..63153818,3	MCF-7	breast:
4	chr1:63079121..63081577-chr1:63084088..63085604,2	MCF-7	breast:
5	chr1:63156083..63158075-chr1:63158423..63161249,2	K562	blood:
6	chr1:63037750..63039379-chr1:63070695..63073673,2	K562	blood:
7	chr1:63063122..63065536-chr1:63066571..63069108,3	K562	blood:
8	chr1:63143255..63144801-chr1:63148236..63149930,2	K562	blood:
9	chr1:63081752..63083296-chr1:63090887..63092573,2	MCF-7	breast:
10	chr1:62991617..62994213-chr1:63008583..63010942,2	K562	blood:
11	chr1:62988619..62991313-chr1:63249394..63251247,2	K562	blood:
12	chr1:62903526..62905902-chr1:62994645..62996175,2	K562	blood:
13	chr1:63151590..63154458-chr1:63248689..63251365,3	K562	blood:
14	chr1:63081404..63083878-chr1:63086190..63087709,2	K562	blood:
15	chr1:63144223..63146231-chr1:63150074..63152820,2	K562	blood:
16	chr1:63102529..63105125-chr5:46100658..46103318,2	MCF-7	breast:
17	chr1:63119431..63121018-chr1:63143900..63145920,2	K562	blood:
18	chr1:63063894..63067391-chr1:63081562..63083857,3	K562	blood:
19	chr1:63141617..63143983-chr1:63151351..63153918,2	MCF-7	breast:
20	chr1:63115924..63118859-chr1:63121146..63123214,2	K562	blood:
21	chr1:63156575..63159018-chr1:63159130..63161249,2	K562	blood:
22	chr1:63081752..63083296-chr1:63090887..63092573,2	MCF-7	breast:
23	chr1:62981414..62983590-chr1:62987870..62990210,2	K562	blood:
24	chr1:63134723..63136885-chr1:63143027..63144543,2	MCF-7	breast:
25	chr1:63003746..63006809-chr1:63007404..63009802,3	K562	blood:
26	chr1:63041177..63043881-chr1:63065271..63067711,2	K562	blood:
27	chr1:62998941..62999670-chr13:28570908..28571561,2	MCF-7	breast:
28	chr1:63088603..63091388-chr1:63093156..63095465,2	K562	blood:
29	chr1:63063122..63065536-chr1:63066571..63069108,3	K562	blood:
30	chr1:63115924..63118859-chr1:63121146..63123214,2	K562	blood:
31	chr1:63146913..63149001-chr1:63152180..63153818,3	MCF-7	breast:
32	chr1:63146446..63150617-chr1:63151147..63154830,6	MCF-7	breast:
33	chr1:63081404..63083878-chr1:63086190..63087709,2	K562	blood:
34	chr1:63012973..63015432-chr1:63018260..63019797,2	K562	blood:
35	chr1:63141617..63143983-chr1:63151351..63153918,2	MCF-7	breast:
36	chr1:63088346..63090747-chr1:63093561..63095201,2	K562	blood:
37	chr1:62996451..62998625-chr1:63013165..63014900,2	K562	blood:
38	chr1:63156575..63159018-chr1:63159130..63161249,2	K562	blood:
39	chr1:63152195..63155380-chr1:63161235..63164349,3	K562	blood:
40	chr1:63088603..63091388-chr1:63093156..63095465,2	K562	blood:
41	chr1:63104828..63107680-chr1:63108196..63110831,3	K562	blood:
42	chr1:62996451..62998625-chr1:63013165..63014900,2	K562	blood:
43	chr1:63151590..63154458-chr1:63248689..63250715,2	K562	blood:
44	chr1:63088346..63090747-chr1:63093561..63095201,2	K562	blood:
45	chr1:63126981..63129509-chr1:63133122..63135258,2	K562	blood:
46	chr1:63156083..63158075-chr1:63158423..63161249,2	K562	blood:
47	chr1:63139232..63141601-chr1:63141772..63144186,2	K562	blood:
48	chr1:63004148..63006809-chr1:63007404..63009476,3	K562	blood:
49	chr1:63062723..63066181-chr1:63069299..63072097,3	K562	blood:
50	chr1:63144223..63146231-chr1:63150074..63152820,2	K562	blood:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ANGPTL3-2	chr1:63139553-63139898	NONHSAT003638
2	lnc-ANGPTL3-2	chr1:63134268-63134368	NONHSAT003638
3	lnc-ANGPTL3-1	chr1:62996307-62996544	NONHSAT003633
4	lnc-USP1-1	chr1:63066705-63066867	NONHSAT003634
5	lnc-KANK4-5	chr1:63142234-63142445	uc_26_-
6	lnc-ANGPTL3-3	chr1:63142234-63142445	uc_26_+
7	lnc-KANK4-6	chr1:63142468-63142757	uc_27_-
8	lnc-USP1-1	chr1:63067956-63068051	NONHSAT003634
9	lnc-USP1-1	chr1:63067440-63067553	NONHSAT003634
10	lnc-ANGPTL3-4	chr1:63142468-63142757	uc_27_+

No data

(count:1 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DOCK7	hsa-miR-30a-5p	chr1:63050383-63050404

Variant related genes	Relation type
ENSG00000269624	TF binding region
DOCK7	TF binding region
ENSG00000235545	TF binding region
ENSG00000213703	TF binding region
ENSG00000270549	TF binding region
ANGPTL3	TF binding region
ENSG00000269624	CpG island
DOCK7	CpG island
ENSG00000235545	CpG island
ENSG00000213703	CpG island
ENSG00000270549	CpG island
ANGPTL3	CpG island
ENSG00000116641	chromatin interactions
ENSG00000235545	chromatin interactions
ENSG00000132855	chromatin interactions
ENSG00000269624	chromatin interactions
ENSG00000213703	chromatin interactions
ENSG00000162607	chromatin interactions
ENSG00000125703	chromatin interactions

Extended variants
information (count: 7230 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:7230 , 50 per page) page: 1 2 3 4 5 6 7 ... 145

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1168043	chr1:62976472-62976473	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs114940878	chr1:62976486-62976487	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs367566871	chr1:62976531-62976532	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs549819084	chr1:62976567-62976568	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571321213	chr1:62976632-62976633	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs538989515	chr1:62976648-62976649	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs192184315	chr1:62976681-62976682	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371363614	chr1:62976734-62976735	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs11207976	chr1:62976751-62976752	Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs149030757	chr1:62976755-62976756	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527633820	chr1:62976773-62976774	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573876103	chr1:62976801-62976802	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs537943259	chr1:62976816-62976817	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556250959	chr1:62976899-62976900	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs12118897	chr1:62976906-62976907	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs6687067	chr1:62976909-62976910	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs534921955	chr1:62976977-62976978	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577578614	chr1:62976989-62976990	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs184737009	chr1:62977000-62977001	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs544959029	chr1:62977133-62977134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs571206388	chr1:62977149-62977150	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs189665110	chr1:62977162-62977163	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs552195018	chr1:62977173-62977174	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572741450	chr1:62977181-62977182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11207977	chr1:62977307-62977308	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
26	rs561151612	chr1:62977325-62977326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs531753257	chr1:62977357-62977358	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs192967118	chr1:62977361-62977362	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs553659090	chr1:62977413-62977414	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1781212	chr1:62977419-62977420	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs184258257	chr1:62977429-62977430	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533960704	chr1:62977483-62977484	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547805904	chr1:62977493-62977494	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs565925191	chr1:62977510-62977511	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs534143504	chr1:62977553-62977554	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1168044	chr1:62977558-62977559	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
37	rs12121689	chr1:62977570-62977571	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144230533	chr1:62977595-62977596	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs544115933	chr1:62977762-62977763	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538002059	chr1:62977769-62977770	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556312595	chr1:62977880-62977881	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs74532324	chr1:62977946-62977947	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs538337642	chr1:62977990-62977991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs553778316	chr1:62977995-62977996	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571901264	chr1:62978019-62978020	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs544781464	chr1:62978037-62978038	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs74076699	chr1:62978157-62978158	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs142602477	chr1:62978223-62978224	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs576254104	chr1:62978244-62978245	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543639911	chr1:62978252-62978253	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Melanoma	18172304	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Rett syndrome	21593744	CNVD
Breast cancer	16620391	CNVD
Prostate cancer	16573809	CNVD
Breast cancer	16608533	CNVD
Ovarian cancer	21720365	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Breast cancer	17133270	CNVD
Myelofibrosis	22110671	CNVD
CNS Malformation Syndrome	17530927	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Type 2 diabetes	21956041	CNVD
Uveal melanoma	20484589	CNVD
Colorectal cancer	20459617	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:3695 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:62909800-62977000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:62916000-62977200	Weak transcription	Right Ventricle	heart
3	chr1:62916600-62976600	Weak transcription	Psoas Muscle	Psoas
4	chr1:62920000-62980200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
5	chr1:62922600-62982000	Weak transcription	A549	lung
6	chr1:62923200-62979200	Weak transcription	Fetal Thymus	thymus
7	chr1:62934400-62981200	Weak transcription	Stomach Mucosa	stomach
8	chr1:62939200-62978200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:62939600-62999800	Weak transcription	Gastric	stomach
10	chr1:62939600-63040600	Weak transcription	Aorta	Aorta
11	chr1:62939800-63044400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr1:62939800-63060200	Weak transcription	Small Intestine	intestine
13	chr1:62941000-63001000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr1:62941600-62978600	Weak transcription	Rectal Smooth Muscle	rectum
15	chr1:62941600-62981400	Weak transcription	Brain Inferior Temporal Lobe	brain
16	chr1:62941600-62998200	Weak transcription	Fetal Heart	heart
17	chr1:62941600-63011800	Weak transcription	Brain Hippocampus Middle	brain
18	chr1:62941800-62978400	Weak transcription	NHEK	skin
19	chr1:62941800-62982000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr1:62941800-62984600	Weak transcription	Brain Cingulate Gyrus	brain
21	chr1:62941800-63030200	Weak transcription	Brain Angular Gyrus	brain
22	chr1:62943600-62979400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chr1:62947200-62978600	Weak transcription	Ovary	ovary
24	chr1:62951200-62980400	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr1:62954000-63003400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr1:62954000-63053400	Weak transcription	Fetal Brain Male	brain
27	chr1:62957200-62977800	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr1:62957800-62998200	Weak transcription	Primary T cells from cord blood	blood
29	chr1:62957800-63050200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr1:62958200-63010800	Weak transcription	Brain Substantia Nigra	brain
31	chr1:62958200-63061000	Weak transcription	Lung	lung
32	chr1:62958400-62984600	Weak transcription	Brain Germinal Matrix	brain
33	chr1:62958400-62997600	Weak transcription	Sigmoid Colon	Sigmoid Colon
34	chr1:62958400-62998200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr1:62958600-62977200	Weak transcription	GM12878-XiMat	blood
36	chr1:62958600-62978200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr1:62960000-62980200	Weak transcription	Colonic Mucosa	Colon
38	chr1:62960000-62998200	Weak transcription	HMEC	breast
39	chr1:62960200-62977800	Weak transcription	Stomach Smooth Muscle	stomach
40	chr1:62960200-62984800	Weak transcription	Primary B cells from cord blood	blood
41	chr1:62960200-62999800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
42	chr1:62960400-62981400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
43	chr1:62960400-62984800	Weak transcription	Duodenum Mucosa	Duodenum
44	chr1:62960400-62985000	Weak transcription	Colon Smooth Muscle	Colon
45	chr1:62960400-62985000	Weak transcription	HSMMtube	muscle
46	chr1:62960400-63004400	Weak transcription	Primary T helper cells fromperipheralblood	blood
47	chr1:62960400-63011800	Weak transcription	Pancreas	Pancrea
48	chr1:62961400-62980400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr1:62961600-62993600	Weak transcription	HUVEC	blood vessel
50	chr1:62961800-62978000	Weak transcription	Primary hematopoietic stem cells short term culture	blood

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